Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
341 to 350 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

341
Clavesin 2
C6orf212, C6orf213, RLBP1L2, bA160A10.4
Hypertension, Myopathy, Schizophrenia

342
Cytochrome c oxidase subunit 7B
APLCC, LSDMCA2
Microphthalmia

343
Cytochrome c oxidase subunit 7C
-
Obesity

344
Cytochrome c oxidase subunit 8A
COX, COX8, COX8-2, COX8L, MC4DN15, VIII, VIII-L
Cytochrome-c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

345
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
MC4DN3
Conotruncal cardiac defect, Cytochrome-c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

346
CD109 molecule
CPAMD7, p180, r150
Basal cell carcinoma, Breast neoplasm, Color vision deficiency, Colorectal neoplasm, Coronary artery disease, Endometriosis, Macular telangiectasia, Multiple sclerosis, Myocardial infarction, Open angle glaucoma, Otosclerosis, Myopia, Uterine fibroid

347
Cytochrome c oxidase assembly factor COX15
CEMCOX2, HAS, MC4DN6
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cardiomyopathy, Cytochrome-c oxidase deficiency, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

348
Ceruloplasmin
AB073614, CP-2
Aceruloplasminemia, Experimental arthritis, Rheumatoid arthritis, Ataxia, Autism, Brain disease, Hepatocellular carcinoma, Colonic neoplasm, Ferroxidase deficiency, Dementia, Diabetes mellitus, Diabetes mellitus type 1, Dyskinesia, Epilepsy, Apoceruloplasmin deficiency
View all (16 more)

349
Carboxypeptidase A1
CPA
Hereditary chronic pancreatitis, Pancreatitis, Diabetes mellitus, type 2

350
Carboxypeptidase A2
-
Hypoxia